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Van Amerongen & Son, Inc.

FDA import alert and refusal historyHagersville, CanadaFEI 1000552474

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Example subjectVan Amerongen & Son, Inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Van Amerongen & Son, Inc. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 27, 2011, was classified VAI (Voluntary Action Indicated).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Van Amerongen & Son, Inc.

2 records, newest first. Each line links to the FDA page it came from.

2017

  1. Recall
    Recall (Class I), Klassic COCONUT DESSICATED COCONUT, 25 LBS. NET, ORGANIC MEDIUM BMO25, PRODUCT OF PHILIPPINESPotential Salmonella contaminaton
    Source

2011

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Van Amerongen & Son, Inc.

Is Van Amerongen & Son, Inc. on an FDA import alert?
No listing for Van Amerongen & Son, Inc. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
Has FDA refused shipments from Van Amerongen & Son, Inc.?
No FDA import refusals for Van Amerongen & Son, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Van Amerongen & Son, Inc. last inspected by FDA?
FDA's most recent inspection of Van Amerongen & Son, Inc. with a final classification is dated May 27, 2011 and was classified VAI (Voluntary Action Indicated).
What is Van Amerongen & Son, Inc.'s FEI number?
Van Amerongen & Son, Inc.'s FDA Establishment Identifier (FEI) is 1000552474.

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Example subjectVan Amerongen & Son, Inc added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.